(19) |
|
|
(11) |
EP 1 368 278 B1 |
(12) |
EUROPEAN PATENT SPECIFICATION |
(45) |
Mention of the grant of the patent: |
|
26.10.2005 Bulletin 2005/43 |
(22) |
Date of filing: 11.03.2002 |
|
(51) |
International Patent Classification (IPC)7: C02F 1/72 |
(86) |
International application number: |
|
PCT/NO2002/000100 |
(87) |
International publication number: |
|
WO 2002/074701 (26.09.2002 Gazette 2002/39) |
|
(54) |
WET OXIDATION WITH THE AID OF A POROUS CATALYTIC CONTACTOR
NASSOXIDATION MIT HILFE EINES PORÖSEN KATALYTISCHEN KONTAKTELEMENTS
OXYDATION EN MILIEU HUMIDE A L'AIDE D'UN CONTACTEUR CATALYTIQUE POREUX
|
(84) |
Designated Contracting States: |
|
AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE TR |
(30) |
Priority: |
12.03.2001 NO 20011238
|
(43) |
Date of publication of application: |
|
10.12.2003 Bulletin 2003/50 |
(73) |
Proprietor: Due Miljo AS |
|
0283 Oslo (NO) |
|
(72) |
Inventors: |
|
- RAEDER, Henrik
N-0851 Oslo (NO)
- BREDESEN, Rune
N-1087 Oslo (NO)
- MIACHON, sylvain
F-69007 Lyon (FR)
- DALMON, Jean-Alain
F-69001 Lyon (FR)
|
(74) |
Representative: Onn, Thorsten et al |
|
Zacco Sweden AB
P.O. Box 23101 104 35 Stockholm 104 35 Stockholm (SE) |
(56) |
References cited: :
EP-A1- 0 887 312
|
US-A- 4 455 236
|
|
|
|
|
|
|
|
|
Note: Within nine months from the publication of the mention of the grant of the European
patent, any person may give notice to the European Patent Office of opposition to
the European patent
granted. Notice of opposition shall be filed in a written reasoned statement. It shall
not be deemed to
have been filed until the opposition fee has been paid. (Art. 99(1) European Patent
Convention).
|
[0001] The present invention relates to a liquid treatment by catalytic oxidation.
[0002] To achieve oxidation of oxidizable, dissolved or suspended substances or particulate
material in a liquid phase, the oxidation process of the present invention utilizes
a catalytic contact element, hereafter called a contactor.
[0003] The primary application of the present invention is to overcome problems associated
with the treatment of industrial waste water and to facilitate the re-use of water,
minerals and other raw materials in industrial processes. In addition, the invention's
process would be useful in breaking down toxic substances and substances that are
not biodegradable. The invention's process makes it possible to achieve oxidation
in the liquid phase at a lower pressure and temperature than what is feasible with
today's processes for wet oxidation and combustion. Also, the process has lower space
requirements than do today's processes for biological treatment of waste. The low
temperature leads to fewer corrosion problems in the processing equipment than with
today's equipment for wet oxidation, enabling the use of less expensive materials.
The result is that the process of the present invention is less demanding with regard
to energy and costs, both for investment and operation, than the current technology.
Furthermore, the present invention's process has a wide range of applications.
[0004] The invention's process would also be useful for purposes other than waste treatment,
for example, for controlled oxidation in the manufacturing of chemicals and products.
[0005] The oxidizable suspended or dissolved material in the liquid may originate from any
source whatsoever. For example, it may be waste water from industry, agriculture or
a similar activity, especially, of course, in those situations where a discharge of
this type of oxidizable material would constitute a strain on, or contamination of,
the exterior environment.
[0006] In given situations, such a process also permits a recovery of the oxidizable material
after the oxidation, and it enables a far greater degree of recycling of purified
waste water instead of discharge.
[0007] The present invention makes use of a technology that utilizes a porous, catalytic
contactor. This porous, catalytic contactor consists essentially of a porous membrane
support that is loaded with a heterogeneous catalyst.
[0008] The porous contactor may consist of one or several layers made of oxides, polymers
or any other materials, and may have any convenient and expedient shape whatsoever,
for example, a tube, a hollow fiber, a multichannel tube, or a plate, or it may have
any other practical form.
[0009] As the catalyst there may be used a precious metal, a non-precious metal, a metal
oxide or any other material. It is also possible that the contactor will not be loaded
with a separate catalytic material, but that the porous membrane material in itself
will have a catalyzing effect for the oxidation reaction.
[0010] In the process according to the invention, one or both of the feed streams can contain
a homogeneous catalyst or one or both of the feed streams can contain a heterogeneous
catalyst.
[0011] Further the catalyst may be supplied batchwise together with either of the two feed
streams or the catalyst may be supplied batchwise during intervals while one or both
of the two feed streams are temporarily stopped.
[0012] The oxidizing phase is a fluid, thus it is a gas or a liquid containing an oxidizing
agent that may be air, oxygen, oxygen-enriched air, ozone, hydrogen peroxide, or another
oxidizing agent.
[0013] The resulting process according to the invention can be carried out in accordance
with various process modes, for example, in batches, by recycling, by continuous feeding
and bleeding, or by a continuous flow-through method.
[0014] In accordance with this the present invention relates to a process for the oxidation
of oxidizable materials which are dissolved or suspended in a liquid phase, and the
invention is characterized in that there is used a contactor in the form of a porous
membrane, said contactor being designed such that an oxidizing phase flows along one
surface of the contactor while the phase to be oxidized flows along the other, and
in that the oxidation is catalysed by (i) a catalyst material which constitutes the
porous membrane or is deposited in or onto a porous membrane support, or catalysed
by (ii) a catalyst material which is supplied to one or both of the feed streams comprising
the oxidizing phase and the phase to the oxidized, respectively, which flow along
said porous membrane support.
[0015] In one embodiment there is as contactor used a porous, ceramic support having a platinum-containing
top layer as catalyst.
[0016] In a further embodiment there is as porous membrane catalyst support used an oxide,
another inorganic material, an organic polymer material or any material.
[0017] The catalyst may be a precious metal, a non-precious metal, an oxide or any other
material.
[0018] The invention shall be described below in more detail with reference to the attached
figures, wherein:
- Figure 1 shows a flow chart for a general apparatus that utilizes the invention's
process;
- Figures 2 and 3 show two examples of the way the catalytic contactor can be arranged
in the reactor in order to utilize the invention's process;
- Figure 4 shows the principle for the oxidation in the catalytic contactor according
to the invention;
- Figure 5 shows a drawing based on a microphotograph in cross section and an embodiment
form of a contactor with a catalyst according to the invention; and
- Figure 6 shows curves illustrating test results obtained through the use of the invention's
process.
[0019] In Figure 1 is shown a flow chart of an apparatus that utilizes the invention's process.
The liquid or suspension to be oxidized enters the pump 2 at 1. The flow rate is regulated
by a valve 3, which is coupled to a flow regulator, and the liquid is conducted into
the reactor 4 on one side of the catalytic contactor 5. The liquid is conducted on
the one side of the contactor, along the contactor's porous surface, and is passed
out of the reactor at 6. The oxidizing agent, which may be air, oxygen, enriched air,
hydrogen peroxide or another oxidizing agent, is introduced at 7 to the pump or the
compressor 8. The flow rate of the oxidizing agent is regulated by a valve 9, which
is coupled to a flow regulator, and the liquid is conducted into the reactor 4 on
the other side of the catalytic contactor 5. The oxidizing agent is conducted on the
other side of the contactor, along the contactor's porous surface, and is passed out
of the reactor at 10. In the illustrated case, the two streams are conducted co-currently
on each side of the porous catalytic contactor, but it is also conceivable that the
two streams can be conducted counter-currently or cross-currently on each side of
the contactor. The pressure conditions in the reactor 4 and the pressure difference
between the two sides of the contactor 5 are regulated by means of valves 11 coupled
to pressure regulators at the outlets from the reactor. The temperature in the reactor
is constantly maintained at the desired level with the aid of a heating/cooling system
12, which may also provide for the recovery of heat. In those cases where the oxidizing
agent is a gas, the outlet from this side of the contactor may be connected to a separator
13, such that any liquid in this outlet can be fed into the oxidized liquid stream
14.
[0020] In Figures 2 and 3 are shown two alternative embodiments of the reactor. Figure 2
shows a reactor composed of a plurality of tubular contactors 20, whereas Figure 3
shows parts of a reactor assembled from a plurality of plate-shaped contactors 30.
The oxidizable liquid is fed in at 21, and the oxidizing agent is introduced at 22.
The oxidized liquid is passed out at 23, whereas unused oxidizing agent and portions
of the oxidation products are removed at 24. Alternatively the streams can be exchanged
such that the oxidizable liquid is introduced at 22 and the oxidizing agent is introduced
at 21. The oxidized liquid is then brought out at 24, whereas unused oxidizing agent
and parts of the oxidation products are passed out at 23.
[0021] Figure 4 illustrates the principle for the invention's mode of operation. In the
porous contactor 40 there is a tone with a material 41 which functions as a catalyst
for the oxidation. The oxidizable material 42, which may be, for example, organic
molecules dissolved in water, is conducted toward the one side of the porous contactor.
The oxidizing agent 43 is conducted in toward the other side of the contactor. The
oxidizable material diffuses into the pores of the contactor, where it meets the oxidizing
agent on, or in the proximity of, the catalyst 41, which causes a spontaneous oxidation
of the oxidizable material to take place. The reaction products 44 and 45 from the
oxidation, which may be in gas or liquid form, diffuse out of the contactor on one
or both of the element's two sides. The reaction products may be completely oxidized
substances, for example, water, carbonates, carbon dioxide or nitrogen oxides, or
partially oxidized substances, for example, carboxylic acids.
[0022] Figure 5 shows a drawing based on a microphotograph of a contactor. In the illustrated
case, the support layer 50 has an average pore diameter in the range 5 to 10 µm to
obtain very weak hydraulic resistance and a thickness of a few mm.
[0023] Onto this support, is laid an intermediary layer 51 in the microfiltration range.
The thickness is around 20 µm.
[0024] Onto this intermediate layer, is laid an additional intermediate layer 52 in the
ultrafiltration range with a thickness around 5 µm. This additional intermediate layer
contains some of the catalyst, in this case platinum. The support layer and the first
intermediate layer do not, in this case, contain catalyst.
[0025] Finally, the contactor comprises a top layer 53 with a thickness around 1 µm. This
layer contains platinum as catalyst.
[0026] Figure 6 shows the results that were obtained through the use of a contactor with
catalyst as shown in Figure 5. The contactor in this case was shaped as a tube having
a length of 100 mm, an outer diameter of 10 mm, and an inner diameter of 6 mm. Figure
5 shows the cross section of an area near the inner surface of a similar tube. The
reactor was utilized with a model solution consisting of 5 g/l of formic acid in water.
A reservoir that contained between 1 and 2 liters of test solution was used for each
test, and the solution was pumped from the reservoir, through the reactor, and back
to the reservoir in a recycling loop. Through the reactor the solution was conducted
along the outside of the contactor tube. The fluid velocity was 50 ml/min. At the
same time, compressed air was conducted through the tube at a velocity of between
50 and 100 ml/min. Samples of the solution were taken from the outlet of the reactor
at irregular intervals. Standard methods for chemical analysis were used to determine
the content of oxidizable material (chemical oxygen demand, COD) or the content of
organic bound carbon (total organic carbon, TOC) in these samples. The results from
these analyses were converted to degree of oxidation by dividing the values by correspondingly
calculated values for the model solution prior to the tests. The degree of oxidation
constitutes the Y-axis in Figure 6. The X-axis represents the time from start of the
test to the time when the sample was taken, divided by the total volume of model solution
in the apparatus at the specified test. In one of the tests, which yielded the results
indicated by the points marked 60 in Figure 6, the pressure in the apparatus was 1
bar and the temperature was 80°C. In another test, which yielded the results indicated
by the points marked 61 in Figure 6, the pressure was 10 bars and the temperature
was 150° C. In both of the tests, the pressure difference between the two sides of
the contactor was less than 0.2 bar.
[0027] The results of the tests that are shown in Figure 6 indicate that it is possible
to achieve over 50% oxidation of formic acid under very mild processing conditions.
Even at a pressure of 1 bar and only 80° C it is possible to achieve nearly 50% oxidation.
In connection with the tests mentioned above, a test was also conducted with a contactor
that was not impregnated with catalyst. This test was carried out at a pressure of
10 bars and a temperature of 150° C, and the results showed that no measurable oxidation
took place in this case.
1. A process for oxidation of oxidizable materials which are dissolved or suspended in
a liquid phase, characterized in that there is used a contactor in the form of a porous membrane, said contactor being
designed such that an oxidizing phase flows along one surface of the contactor while
the phase to be oxidized flows along the other, and in that the oxidation is catalysed by (i) a catalyst material which constitutes the porous
membrane or is deposited in or onto a porous membrane support, or catalysed by (ii)
a catalyst material which is supplied to one or both of the feed streams comprising
the oxidizing phase and the phase to the oxidized, respectively, which flow along
said porous membrane support.
2. The process according to claim 1, characterized in that as contactor there is used a porous, ceramic support having a platinum-containing
top layer as catalyst.
3. The process according to claims 1 or 2, characterized in that as oxidizing agent there is used air, oxygen-enriched air, oxygen, ozone, hydrogen
peroxide or any other oxidizing substance whatsoever.
4. The process according to any one of the preceding claims, characterized in that the contactor has the shape of a tube, a hollow fiber, a multichannel tube, a plate
or any other form.
5. The process according to any one of the preceding claims, characterized in that as a porous membrane catalyst support there is used an oxide, another inorganic material,
an organic polymer material or any other material.
6. The process according to any one of the preceding claims, characterized in that as catalyst there is used a precious metal, a non-precious metal, an oxide or any
other material.
7. The process according to any one of the preceding claims, characterized in that one or both of the feed streams contain a heterogeneous catalyst.
8. The process according to any one of the preceding claims, characterized in that one or both of the feed streams contain a homogeneous catalyst.
9. The process according to any one of the preceding claims, characterized in that the catalyst is supplied batchwise together with either of the two feed streams.
10. The process according to any one of the preceeding claims, characterized in that the catalyst is supplied batchwise during intervals while one or both of the two
feed streams are temporarily stopped.
1. Verfahren zur Oxidation von oxidierbaren Stoffen, welche in einer Flüssigphase gelöst
oder suspendiert sind, dadurch gekennzeichnet, dass ein Kontaktelement in Form einer porösen Membran verwendet wird, wobei das Kontaktelement
derart ausgebildet ist, dass eine oxidierende Phase auf der einen Seite des Kontaktelements
entlangströmt und die zu oxidierende Phase auf der anderen Seite, und dass die Oxidation
katalysiert wird durch (i) ein Katalysatormaterial, welches die poröse Membran bildet
oder in oder auf einem Träger der porösen Membran abgelagert ist, oder durch (ii)
ein Katalysatormaterial, welches einem oder beiden der die oxidierende Phase bzw.
die zu oxidierende Phase enthaltenden Zufuhrströme zugegeben wird, die dem Träger
der genannten porösen Membran entlang strömen.
2. Verfahren nach Anspruch 1, dadurch gekennzeichnet, dass als Kontaktelement ein poröser keramischer Träger verwendet wird mit einer platinhaltigen
Deckschicht als Katalysator.
3. Verfahren nach Anspruch 1 oder 2, dadurch gekennzeichnet, dass als Oxidationsmittel Luft, mit Sauerstoff angereicherte Luft, Sauerstoff, Ozon, Wasserstoffperoxid
oder ein beliebiger anderer oxidierender Stoff verwendet wird.
4. Verfahren nach einem der vorangehenden Ansprüche, dadurch gekennzeichnet, dass das Kontaktelement die Form einer Röhre, einer Hohlfaser, eines Vielkanalrohrs ,
einer Platte oder eine beliebige andere Form aufweist.
5. Verfahren nach einem der vorangehenden Ansprüche, dadurch gekennzeichnet, dass als Träger der porösen Katalysatormembran ein Oxid, ein anderes anorganisches Material,
ein organisches Polymermaterial oder ein beliebiges anderes Material verwendet wird.
6. Verfahren nach einem der vorangehenden Ansprüche, dadurch gekennzeichnet, dass als Katalysator ein Edelmetall, ein Nichtedelmetall, ein Oxid oder ein beliebiges
anderes Material verwendet wird.
7. Verfahren nach einem der vorangehenden Ansprüche, dadurch gekennzeichnet, dass einer der Zufuhrstöme oder beide einen heterogenen Katalysator enthält/enthalten.
8. Verfahren nach einem der vorangehenden Ansprüche, dadurch gekennzeichnet, dass einer der Zufuhrstöme oder beide einen homogenen Katalysator enthält/enthalten.
9. Verfahren nach einem der vorangehenden Ansprüche, dadurch gekennzeichnet, dass der Katalysator chargenweise zusammen mit einem der beiden Zufuhrströme zugegeben
wird.
10. Verfahren nach einem der vorangehenden Ansprüche, dadurch gekennzeichnet, dass der Katalysator chargenweise in Intervallen zugegeben wird, während denen einer der
beiden Zufuhrstöme oder beide vorübergehend unterbrochen sind.
1. Procédé d'oxydation de matières oxydables dissoutes ou suspendues dans une phase liquide,
caractérisé en ce qu'un contacteur sous forme d'une membrane poreuse est utilisé, ledit contacteur étant
conçu de sorte qu'une phase oxydante s'écoule le long d'une surface du contacteur
alors que la phase à oxyder s'écoule le long de l'autre, et en ce que l'oxydation est catalysée par (i) un matériau catalyseur qui constitue la membrane
poreuse ou est déposé dans ou sur un support de la membrane poreuse, ou catalysée
par (ii) un matériau catalyseur qui est alimenté à l'un ou aux deux flux d'alimentation
comprenant la phase oxydante et la phase à oxyder, respectivement, qui s'écoulent
le long dudit support de la membrane poreuse.
2. Procédé selon la revendication 1, caractérisé en ce que comme contacteur est utilisé un support poreux en céramique muni d'une couche de
surface contenant du platine comme catalyseur.
3. Procédé selon les revendications 1 ou 2, caractérisé en ce que comme agent oxydant est utilisé de l'air, de l'air enrichi en oxygène, de l'oxygène,
de l'ozone, du peroxide d'hydrogène ou toute autre substance oxydante quelconque.
4. Procédé selon l'une quelconque des revendications précédentes, caractérisé en ce que le contacteur présente la forme d'un tube, d'une fibre creuse, d'un tube à canaux
multiples, d'une plaque ou toute autre forme.
5. Procédé selon l'une quelconque des revendications précédentes, caractérisé en ce que comme support de la membrane catalytique poreuse est utilisé un oxyde, une autre
matière inorganique, une matière polymère organique ou toute autre matière.
6. Procédé selon l'une quelconque des revendications précédentes, caractérisé en ce que comme catalyseur est utilisé un métal précieux, un métal non précieux, un oxyde ou
tout autre matériau.
7. Procédé selon l'une quelconque des revendications précédentes, caractérisé en ce que l'un ou les deux flux d'alimentation contient/contiennent un catalyseur hétérogène.
8. Procédé selon l'une quelconque des revendications précédentes, caractérisé en ce que l'un ou les deux flux d'alimentation contient/contiennent un catalyseur homogène.
9. Procédé selon l'une quelconque des revendications précédentes, caractérisé en ce que le catalyseur est alimenté en discontinu avec l'un des deux flux d'alimentation.
10. Procédé selon l'une quelconque des revendications précédentes, caractérisé en ce que le catalyseur est alimenté en discontinu pendant des intervalles où l'un ou les deux
flux d'alimentation sont temporairement arrétés.